NM_017882.3(CLN6):c.831C>T (p.Val277=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jun 23, 2015
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001655622.2
Allele description [Variation Report for NM_017882.3(CLN6):c.831C>T (p.Val277=)]
NM_017882.3(CLN6):c.831C>T (p.Val277=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024